A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694407



Internal ID15431059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121566328..121734858hg38UCSC Ensembl
InnerchrX:120700182..120868711hg19UCSC Ensembl
InnerchrX:120527863..120696392hg18UCSC Ensembl
InnerchrX:120425717..120594246hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38168531
hg19168530
hg18168530
hg17168530
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520918
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694407
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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